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RDDpred: a condition-specific RNA-editing prediction model from RNA-seq data

DC Field Value Language
dc.contributor.authorKim, Min-su-
dc.contributor.authorHur, Benjamin-
dc.contributor.authorKim, Sun-
dc.date.accessioned2017-02-07T06:29:54Z-
dc.date.available2017-02-07T06:29:54Z-
dc.date.issued2016-01-11-
dc.identifier.citationBMC Genomics, 17(Suppl 1):5ko_KR
dc.identifier.urihttps://hdl.handle.net/10371/100485-
dc.descriptionThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any
medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons
license, and indicate if changes were made.
ko_KR
dc.description.abstractAbstract

Background
RNA-editing is an important post-transcriptional RNA sequence modification performed by two catalytic enzymes, "ADAR"(A-to-I) and "APOBEC"(C-to-U). By utilizing high-throughput sequencing technologies, the biological function of RNA-editing has been actively investigated. Currently, RNA-editing is considered to be a key regulator that controls various cellular functions, such as protein activity, alternative splicing pattern of mRNA, and substitution of miRNA targeting site. DARNED, a public RDD database, reported that there are more than 300-thousands RNA-editing sites detected in human genome(hg19). Moreover, multiple studies suggested that RNA-editing events occur in highly specific conditions. According to DARNED, 97.62 % of registered editing sites were detected in a single tissue or in a specific condition, which also supports that the RNA-editing events occur condition-specifically. Since RNA-seq can capture the whole landscape of transcriptome, RNA-seq is widely used for RDD prediction. However, significant amounts of false positives or artefacts can be generated when detecting RNA-editing from RNA-seq. Since it is difficult to perform experimental validation at the whole-transcriptome scale, there should be a powerful computational tool to distinguish true RNA-editing events from artefacts.


Result
We developed RDDpred, a Random Forest RDD classifier. RDDpred reports potentially true RNA-editing events from RNA-seq data. RDDpred was tested with two publicly available RNA-editing datasets and successfully reproduced RDDs reported in the two studies (90 %, 95 %) while rejecting false-discoveries (NPV: 75 %, 84 %).


Conclusion
RDDpred automatically compiles condition-specific training examples without experimental validations and then construct a RDD classifier. As far as we know, RDDpred is the very first machine-learning based automated pipeline for RDD prediction. We believe that RDDpred will be very useful and can contribute significantly to the study of condition-specific RNA-editing. RDDpred is available at

http://biohealth.snu.ac.kr/software/RDDpred


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ko_KR
dc.language.isoenko_KR
dc.publisherBioMed Centralko_KR
dc.subjectRNA-editingko_KR
dc.subjectCondition-specificko_KR
dc.subjectMachine-learningko_KR
dc.subjectRandom forestko_KR
dc.subjectRNA-seqko_KR
dc.subjectSystematic artefactko_KR
dc.titleRDDpred: a condition-specific RNA-editing prediction model from RNA-seq datako_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor김민수-
dc.contributor.AlternativeAuthor허벤자민-
dc.contributor.AlternativeAuthor김선-
dc.identifier.doi10.1186/s12864-015-2301-y-
dc.language.rfc3066en-
dc.rights.holderKim et al.-
dc.date.updated2017-01-06T10:07:51Z-
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